Changes in histopathology and heteroplasmy rates over 8 years and effectiveness of taurine supplementation in a patient with mitochondrial nephropathy caused by MT-TL1 mutation: A case report

Author:

Imasawa ToshiyukiORCID,Kitamura Hiroshi,Kawaguchi Takehiko,Yatsuka YukikoORCID,Okazaki Yasushi,Murayama Kei

Funder

Japan Agency for Medical Research and Development

Publisher

Elsevier BV

Subject

Multidisciplinary

Reference16 articles.

1. Mitochondrial encephalomyopathies preceded by de-Toni-Debré-Fanconi syndrome or focal segmental glomerulosclerosis;Mochizuki;Clin. Nephrol.,1996

2. Clinical and pathologic features of focal segmental glomerulosclerosis with mitochondrial tRNALeu (UUR) gene mutation;Hotta;Kidney Int.,2001

3. Clinicopathologic features of mitochondrial nephropathy;Imasawa;Kidney Int. Rep.,2022

4. Podocyte energy metabolism and glomerular diseases;Imasawa;Int. J. Biochem. Cell Biol.,2013

5. The dynamics of mitochondrial DNA heteroplasmy: implications for human health and disease;Stewart;Nat. Rev. Genet.,2015

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